CClinicalTrials.gg
CompletedNCT02714517Updated Sep 30, 2016

Efficacy of Hydrotherapy in Peripheral Neuropathy

An interventional study of hydrotherapy and on land therapy in Peripheral Neuropathy, sponsored by Ospedale Generale Di Zona Moriggia-Pelascini. Completed at 1 site in Italy. Open to participants aged 18 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-09-30.

Sponsored by Ospedale Generale Di Zona Moriggia-Pelascini · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The purpose of the study is to evaluate the efficacy of hydrotherapy on pain and balance in patients affected by neuropathy.

02

Conditions studied

  • Peripheral Neuropathy
03

In context

Peripheral Nervous System Diseases

1,003 studies on the registry are indexed under Peripheral Nervous System Diseases; 177 are open to participants now.

This study's enrollment of 40 is below the median of 60 across 768 interventional studies indexed under Peripheral Nervous System Diseases.

Browse Peripheral Nervous System Diseases studies →

Lead sponsor

Ospedale Generale Di Zona Moriggia-Pelascini is the lead sponsor of 36 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • patients affected by peripherical neuropathy able to walk

Exclusion criteria

Exclusion Criteria:

  • pain of water
  • medical contraindications at treatment in heated swimming pool
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    hydrotherapy

    patients receive daily conventional physiotherapy and three 30- minutes sessions of in- water exercises per week, for four weeks

    Other: hydrotherapy

  • Active comparator
    controls

    patients receive daily conventional physiotherapy and three 30- minutes sessions of on- land exercises per week, for four weeks

    Other: on land therapy

Interventions

  • Otherhydrotherapy

    30 minutes sessions of physiotherapy exercises in heated pool (32°C), three times per week for four weeks

  • Otheron land therapy

    30 minutes sessions of physiotherapy exercises on land, three times per week for four weeks

06

What researchers measure

Primary outcomes

  1. balance change assessed using Berg Balance Scale

    Time frame: 0 and 4 weeks

  2. disability change assessed using Functional Independence Measure scale

    Time frame: 0 and 4 weeks

  3. gait change assessed using Dynamic Gait Index scale

    Time frame: 0 and 4 weeks

  4. gait change assessed using Functional Ambulation Classification scale

    Time frame: 0 and 4 weeks

  5. pain change assessed using Overall Neuropathy Limitation Scale

    Time frame: 0 and 4 weeks

  6. disability change assessed using Neuropathy Pain Scale

    Time frame: 0 and 4 weeks

07

Study locations

1 site
  • Ospedale generale di zona Moriggia Pelascini
    Gravedona ed Uniti, CO 22015, Italy
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 30, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02714517
Lead sponsor
Ospedale Generale Di Zona Moriggia-Pelascini
Responsible party
Ilaria Zivi (MD, Ospedale Generale Di Zona Moriggia-Pelascini) — Principal investigator
First posted
Mar 21, 2016
Start date
Jul 2015
Primary completion
Jun 2016
Last update
Sep 30, 2016
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion